Charron J, Malynn B A, Robertson E J, Goff S P, Alt F W
Howard Hughes Medical Institute, New York, New York.
Mol Cell Biol. 1990 Apr;10(4):1799-804. doi: 10.1128/mcb.10.4.1799-1804.1990.
Identification of gene function has often relied on isolation of mutant cells in which expression of the gene was inactivated. Gene targeting by homologous recombination in tissue culture now may provide a technology to rapidly and directly produce such mutant mammalian cells. We demonstrate that selection of embryonic stem and pre-B cell lines for expression of a promoterless construct containing murine N-myc genomic sequences fused to a gene encoding neomycin resistance allows highly efficient recovery of variants in which the endogenous N-myc gene is disrupted. The high frequency of N-myc gene disruption by this method should permit targeted disruption of both allelic N-myc copies in various cell lines to study N-myc function.
基因功能的鉴定通常依赖于分离基因表达被灭活的突变细胞。组织培养中通过同源重组进行基因打靶现在可能提供一种技术,以快速直接地产生此类突变的哺乳动物细胞。我们证明,选择胚胎干细胞和前B细胞系来表达一个无启动子构建体,该构建体包含与编码新霉素抗性的基因融合的鼠N-myc基因组序列,能够高效回收内源性N-myc基因被破坏的变体。通过这种方法N-myc基因的高破坏频率应能使各种细胞系中的两个等位N-myc拷贝都被靶向破坏,从而研究N-myc的功能。